Toxic shock syndrome and bacterial superantigens: An update

被引:512
作者
McCormick, JK [1 ]
Yarwood, JM [1 ]
Schlievert, PM [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
关键词
Staphylococcus aureus; Streptococcus pyogenes; hypotension; T cell stimulation;
D O I
10.1146/annurev.micro.55.1.77
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Toxic shock syndrome (TSS) is an acute onset illness characterized by fever, rash formation, and hypotension that can lead to multiple organ failure and lethal shock, as well as desquamation in patients that recover. The disease is caused by bacterial superantigens (SAGs) secreted from Staphylococcus aureus and group A streptococci. SAGs bypass normal antigen presentation by binding to class II major histocompatibility complex molecules on antigen-presenting cells and to specific variable regions on the beta -chain of the T-cell antigen receptor. Through this interaction, SAGs activate T cells at orders of magnitude above antigen-specific activation, resulting in massive cytokine release that is believed to be responsible for the most severe features of TSS. This review focuses on clinical and epidemiological aspects of TSS, as well as important developments in the genetics, biochemistry, immunology, and structural biology of SAGs. From the evolutionary relationships between these important toxins, we propose that there are five distinct groups of SAGs.
引用
收藏
页码:77 / 104
页数:32
相关论文
共 179 条
[1]   STRUCTURAL BASIS OF SUPERANTIGEN ACTION INFERRED FROM CRYSTAL-STRUCTURE OF TOXIC-SHOCK SYNDROME TOXIN-1 [J].
ACHARYA, KR ;
PASSALACQUA, EF ;
JONES, EY ;
HARLOS, K ;
STUART, DI ;
BREHM, RD ;
TRANTER, HS .
NATURE, 1994, 367 (6458) :94-97
[2]   Role of the T cell receptor α chain in stabilizing TCR-superantigen-MHC class II complexes [J].
Andersen, PS ;
Lavoie, PM ;
Sékaly, RP ;
Churchill, H ;
Kranz, DM ;
Schlievert, PM ;
Karjalainen, K ;
Mariuzza, RA .
IMMUNITY, 1999, 10 (04) :473-483
[3]   Superantigen antagonist protects against lethal shock and defines a new domain for T-cell activation [J].
Arad, G ;
Levy, R ;
Hillman, D ;
Kaempfer, R .
NATURE MEDICINE, 2000, 6 (04) :414-421
[4]   Conservation and variation in superantigen structure and activity highlighted by the three-dimensional structures of two new superantigens from Streptococcus pyogenes [J].
Arcus, VL ;
Proft, T ;
Sigrell, JA ;
Baker, HM ;
Fraser, JD ;
Baker, EN .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 299 (01) :157-168
[5]   Cutting edge: Cell autonomous rather than environmental factors control bacterial superantigen-induced T cell anergy in vivo [J].
Attinger, A ;
Acha-Orbea, H ;
MacDonald, HR .
JOURNAL OF IMMUNOLOGY, 2000, 165 (03) :1171-1174
[6]   NONSPECIFIC AND SPECIFIC IMMUNOLOGICAL MITOGENICITY BY GROUP-A STREPTOCOCCAL PYROGENIC EXOTOXINS [J].
BARSUMIAN, EL ;
SCHLIEVERT, PM ;
WATSON, DW .
INFECTION AND IMMUNITY, 1978, 22 (03) :681-688
[7]   Opsonic antibodies to the surface M protein of group A streptococci in pooled normal immunoglobulins (IVIG): Potential impact on the clinical efficacy of IVIG therapy for severe invasive group a streptococcal infections [J].
Basma, H ;
Norrby-Teglund, A ;
McGeer, A ;
Low, DE ;
El-Ahmedy, O ;
Dale, JB ;
Schwartz, B ;
Kotb, M .
INFECTION AND IMMUNITY, 1998, 66 (05) :2279-2283
[8]  
Basma H, 1999, INFECT IMMUN, V67, P1871
[9]   GENETIC AND MOLECULAR ANALYSES OF THE GENE ENCODING STAPHYLOCOCCAL ENTEROTOXIN-D [J].
BAYLES, KW ;
IANDOLO, JJ .
JOURNAL OF BACTERIOLOGY, 1989, 171 (09) :4799-4806
[10]   GROUP-A BETA-HEMOLYTIC STREPTOCOCCAL TOXIC SHOCK-LIKE SYNDROME [J].
BEGOVAC, J ;
MARTON, E ;
LISIC, M ;
BEUS, I ;
BOZINOVIC, D ;
KUZMANOVIC, N .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1990, 9 (05) :369-370